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Details
Link-It Detail - Jax Mouse Phenotype - abnormal mitochondrial inner membrane morphology
Debug Stats
  • ### Total Build Time: 19 ms 16.556 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 424 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 293 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 206 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 588 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 597 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.573 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=9 ms Completed: 9 ms rowSize= 11.594 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.186 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal mitochondrial inner membrane morphology MP:0011634
Definition (1)
any structural anomaly of the inner, i.e. lumen-facing, lipid bilayer of the mitochondrial envelope, which is highly folded to form cristae
Synonyms (1)
"abnormal inner mitochondrial membrane morphology" EXACT
Parents (1)
img abnormal mitochondrion morphology MP:0006035
Children (1)
img abnormal mitochondrial crista morphology MP:0011635
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cellular phenotype MP:00053845img abnormal mitochondrion morphology MP:0006035
Genes (21)

Species:
human : 21
SpeciesGeneGeneIdGene NameEvidence
HumanCISD2493856CDGSH iron sulfur domain 2
INFERRED
HumanRNASEH1246243ribonuclease H1
INFERRED
HumanPNPT187178polyribonucleotide nucleotidyltransferase 1
INFERRED
HumanNOA184273nitric oxide associated 1
INFERRED
HumanCHDH55349choline dehydrogenase
INFERRED
HumanNDUFA1351079NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 13
INFERRED
HumanPOLG211232polymerase (DNA directed), gamma 2, accessory subunit
INFERRED
HumanAIFM19131apoptosis-inducing factor, mitochondrion-associated, 1
INFERRED
HumanSQSTM18878sequestosome 1
INFERRED
HumanHDAC38841histone deacetylase 3
INFERRED
HumanPLA2G68398phospholipase A2, group VI (cytosolic, calcium-independent)
INFERRED
HumanVCP7415valosin containing protein
INFERRED
HumanTK27084thymidine kinase 2, mitochondrial
INFERRED
HumanTFAM7019transcription factor A, mitochondrial
INFERRED
HumanSLC8A16546solute carrier family 8 (sodium/calcium exchanger), member 1
INFERRED
HumanPEX55830peroxisomal biogenesis factor 5
img Jax MP, Pubmed Id: 15732085, MOUSE PHENOTYPE ID: MGI:1098808
img Jax MP, Pubmed Id: 22881289, MOUSE PHENOTYPE ID: MGI:5462362
HumanPEX135194peroxisomal biogenesis factor 13
INFERRED
HumanOPA14976optic atrophy 1 (autosomal dominant)
INFERRED
HumanNDUFS44724NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase)
INFERRED
HumanMPV174358MpV17 mitochondrial inner membrane protein
INFERRED
HumanCD44960CD44 molecule (Indian blood group)
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0011634abnormal mitochondrial inner membrane morphology0self